Canonical Allele Identifier: CA1821104962

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133625G= , CM000670.2:g.133133625G=	GRCh38
NC_000008.10:g.134145869G= , CM000670.1:g.134145869G=	GRCh37
NC_000008.9:g.134215051G=	NCBI36
NG_015832.1:g.271665G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8153G= MANE Select	ENSP00000220616.4:p.Trp2718=
ENST00000220616.8:c.8153G=	ENSP00000220616.4:p.Trp2718=
ENST00000519178.5:c.3519G=
ENST00000519543.5:c.2552G=	ENSP00000430430.1:p.Trp851=
ENST00000521107.1:c.365G=	ENSP00000430161.1:p.Trp122=
ENST00000522691.1:n.239G=
ENST00000523756.5:c.4808G=
NM_003235.4:c.8153G=	NP_003226.4:p.Trp2718=
XM_005251038.3:c.7961G=	XP_005251095.1:p.Trp2654=
XM_006716622.2:c.8090G=	XP_006716685.1:p.Trp2697=
XM_005251038.4:c.7961G=	XP_005251095.1:p.Trp2654=
XM_006716622.3:c.8090G=	XP_006716685.1:p.Trp2697=
XM_017013793.1:c.8087G=	XP_016869282.1:p.Trp2696=
XM_017013794.1:c.8018G=	XP_016869283.1:p.Trp2673=
XM_017013795.1:c.7982G=	XP_016869284.1:p.Trp2661=
XM_017013796.1:c.7934G=	XP_016869285.1:p.Trp2645=
XM_017013797.1:c.7892G=	XP_016869286.1:p.Trp2631=
NM_003235.5:c.8153G= MANE Select	NP_003226.4:p.Trp2718=